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Browse result for Primary hyperoxaluria
※ introduction Primary hyperoxaluria is a rare condition (autosomal recessive), resulting in increased excretion of oxalate (up to 600 mg a day from normal 50 mg a day), with oxalate stones being common.
Reference
Wiki: Primary hyperoxaluria
Reference
Wiki: Primary hyperoxaluria
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD04477 | P21549 | 189 | AGXT | Alanine--glyoxylate aminotransferase | Homo sapiens |
| PTMD14017 | Q9UBQ7 | 9380 | GRHPR | Glyoxylate reductase/hydroxypyruvate reductase | Homo sapiens |
